Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
  • A61P33/10—Anthelmintics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
  • A61P33/14—Ectoparasiticides, e.g. scabicides
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems

Definitions

• This invention relates to imidazoles having parasiticidal properties.
• the compounds of interest are substituted imidazoles and, more particularly, the invention relates to alpha substituted 2-benzyl imidazoles.
• antiparasitic agents for use with mammals, including humans and animals, and in particular there is a need for improved insecticides and acaricides.
• topical products with convenient administration and which contain one or more of such antiparasitic agents which can be used to effectively treat ectoparasites, such as insects and acarids, and particularly aracids such as mites and ticks.
• ectoparasites such as insects and acarids, and particularly aracids such as mites and ticks.
• Such products would be particularly useful for the treatment of companion animals, such as cats, dogs and horses, and livestock, such as cattle.
• agents to control parasitic infestations in animal hosts other than mammals including insects such as bees, which are susceptible to parasites such as varroa mites.
• the compounds currently available for insecticidal and acaricidal treatment of companion animals and livestock do not always demonstrate good activity, good speed of action, or a long duration of action. Most treatments contain hazardous chemicals that can have serious consequences when either used too often or when used in excess of recommended quantities. Many products have toxic side effects and some are lethal to cats when accidentally ingested. They are not always suitable for use as a topical or spot-on formulation and some topical and spot-on formulations are disadvantaged by common side effects in animals and owners. Persons applying these insecticidal and acaricidal agents are advised to limit their exposure to the chemicals by wearing gloves and avoiding inhalation of the chemical vapours.
• Pet collars and tags have been utilised to overcome some problems, but these are susceptible to chewing and therefore are disadvantageous since the compound may be accidentally orally ingested.
• treatments currently achieve varying degrees of success depending on a variety of factors including toxicity and the method of administration. In some cases toxicity may be attributed to their non-selective activity at various receptors. In addition it has recently been shown that some current agents are becoming ineffective as the parasites develop resistance.
• the present invention overcomes one or more of the various disadvantages of, or improves upon, the properties of existing compounds.
• the present invention develops some new alpha substituted 2-benzyl imidazoles which demonstrate such properties.
• Heterocyclic derivatives have been disclosed in the prior art as having insecticidal and acaricidal activity against agricultural pests, for example International patent application publication no. WO 03/092374.
• Pat. No. 6,103,733 describes a generic structure which optionally encompasses alpha substituted 2-benzyl imidazoles for increasing blood serum and HDL cholesterol levels.
• none of this prior art exemplifies any alpha substituted 2-benzyl imidazoles, nor does the prior art indicate that such compounds would be useful against a spectrum of parasites relevant to companion animals and livestock or against the range of ectoparasite lifecycle stages.
• it is a further aim that such new compounds have the same or improved activity when compared to the prior art compounds against parasites.
• the invention is an aim of the invention to reduce the exposure of both humans and animals to the treatment by developing compounds which can be dosed as a low volume spot-on or topical application.
• the compounds of the present invention have especially good ability to control arthropods as shown by the results of tests demonstrating their potency and efficacy.
• the compounds of the present invention are active against ticks and they are able to prevent ticks from attaching to, and feeding from, the host animal.
• the compounds of the present invention should have one or more of the same or improved duration of action, an improved pharmacokinetic profile, improved safety, improved persistence, improved solubility or other improved physicochemical and formulation properties such as good spreading after topical application compared to those of the prior art.
• C 1-4 alkyl optionally substituted by one or more hydroxy groups means an alkyl group with between one and four carbon atoms, which may be unsubstituted or may be substituted at any available position with a hydroxy group. For reasons of chemical stability, it is preferred that no carbon atom should be substituted with more than one hydroxy group. Accordingly, alkyl groups with up to four hydroxy substituents are foreseen. Preferred are alkyl groups with no more than two hydroxy substituents. Examples include hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1,2-dihydroxyethyl and 2,3-dihydroxypropyl.
• C 3-6 cycloalkyl optionally substituted by one or more C 1-4 alkyl or halo groups means a cycloalkyl group with between three and six carbon atoms in the ring, which may be unsubstituted or may be substituted at any available position with an alkyl group of between one and four carbon atoms or a halogen atom.
• alkyl substituents it is preferred that not more than four such substituents be present, and more preferred that not more than two such substituents be present.
• Examples include 1-methylcyclopropyl, 2,5-dimethylcyclopentyl and 4-tert-butylcyclohexyl.
• any degree of substitution up to complete substitution is foreseen.
• cyclohexyl therefore, up to eleven halo substituents may be present. While each halo group may be independently selected, it may be preferred to have all halo substituents the same. Preferably the halo is chloro or fluoro. Geminal disubstitution at any methylene position may be preferred ver monosubstitution. Examples include 2,2-dichlorocyclopropyl and perfluorocyclohexyl. Substitution with both alkyl and halo groups is also foreseen. An example is 2,2-difluoro-1-methylcyclobutyl.
• each of R 1 , R 2 , R 3 , R 4 , R 5 are independently selected from hydrogen, halo eg chloro or fluoro, C 1-4 alkyl eg methyl or ethyl, C 3-4 cycloalkyl eg cyclopropyl, C 1-4 alkoxy eg methoxy or ethoxy, C 1-4 haloalkyl eg trifluoromethyl, trifluoroethyl, C 1-4 haloalkoxy eg trifluoromethoxy or trifluoroethoxy, and S(O) n R 10 where n is 0 and R 10 is preferably selected from C 1-4 alkyl such as methyl or ethyl or C 1-4 haloalkyl such as trifluoromethyl or trifluoroethyl to form for example trifluoromethylthio or trifluoroethylthio.
• each of R 1 , R 2 , R 3 , R 4 , R 5 are independently selected from hydrogen, halo eg chloro, C 1-4 alkyl eg methyl or ethyl, C 1-4 alkoxy eg methoxy or ethoxy, and C 1-4 haloalkyl eg trifluoromethyl, trifluoroethyl.
• R 1 , R 2 , R 3 , R 4 , R 5 are independently selected from hydrogen, and C 1-4 alkyl eg methyl or ethyl.
• R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from C 1-4 alkyl eg methyl or ethyl, preferably methyl, and three of R 1 , R 2 , R 3 , R 4 , and R 5 are H. Even more preferably R 1 and R 2 are selected from C 1-4 alkyl eg methyl or ethyl, preferably methyl, and R 3 , R 4 and R 5 are H.
• R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from C 1-4 haloalkyl eg trifluoromethyl, trifluoroethyl, preferably trifluoromethyl, with the others of R 1 , R 2 , R 3 , R 4 , and R 5 being H.
• R 2 is C 1-4 haloalkyl eg trifluoromethyl, trifluoroethyl preferably trifluoroethyl, with the others of R 1 , R 3 , R 4 , and R 5 being H.
• R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from C 1-4 alkoxy eg methoxy or ethoxy preferably methoxy, with the others of R 1 , R 2 , R 3 , R 4 , and R 5 being H.
• R 2 and R 3 are selected from C 1-4 alkoxy eg methoxy or ethoxy preferably methoxy, and R 1 , R 4 and R 5 are H.
• R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from halo eg chloro or fluoro, with the others of R 1 , R 2 , R 3 , R 4 , and R 5 being H.
• R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from halo eg chloro or fluoro, and another one of R 1 , R 2 , R 3 , R 4 , and R 5 is independently selected from C 1-4 alkyl eg methyl or ethyl, with the others of R 1 , R 2 , R 3 , R 4 , and R 5 being H.
• R 1 and R 2 are methyl and R 3 , R 4 , and R 5 are hydrogen.
• R 6 is selected from the group consisting of hydrogen; —C 0-2 alkyleneR 7 ; —C 1-2 alkyleneOR 7 ; —C 1-2 alkyleneOC(O)R 7 ; —C 1-2 alkyleneOC(O)OR 7 ; —C 0-2 alkyleneC(O)OR 7 ; —C 1-2 alkyleneOC(O)NHR 7 ; —C 1-2 alkyleneOC(O)NR 15 R 16 ; and —C 0-2 alkyleneS(O) n R 10 .
• R 6 is selected from the group consisting of hydrogen; —C 0-2 alkyleneR 7 ; —C 1-2 alkyleneOR 7 ; —C 1-2 alkyleneOC(O)R 7 ; —C 1-2 alkyleneOC(O)OR 7 ; and —C 0-2 alkyleneC(O)OR 7 .
• R 5 is selected from the group consisting of hydrogen; —C 0-2 alkyleneR 7 ; —C 1-2 alkyleneOC(O)R 7 and —C 0-2 alkyleneC(O)OR 7 .
• R 6 is hydrogen.
• R 7 , R 15 and R 16 are, where chemically possible, independently selected from the group consisting of hydrogen; C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl; C 3-8 cycloalkyl for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl; C 1-4 alkylene(C 3-6 cycloalkyl) for example cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclohexylmethyl, cyclohexylethyl; C 1-6 haloalkyl for example fluoromethyl, trifluoromethyl, chloromethyl, fluoro
• R 7 , R 15 and R 16 are, where chemically possible, independently selected from the group consisting of hydrogen; C 1-6 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, n-pentyl, n-hexyl; C 1-4 alkylene(C 3-6 cycloalkyl) for example cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclohexylmethyl, cyclohexylethyl.
• R 7 , R 15 and R 16 are, where chemically possible, independently selected from the group consisting of hydrogen and C 1-4 alkyl for example methyl, ethyl, propyl, isopropyl, n-butyl and tert-butyl.
• R 7 , R 15 and R 16 are, where chemically possible, optionally substituted with one or more substituents selected from the group consisting of halo for example fluoro or chloro, C 1-4 alkyl for example methyl or ethyl preferably methyl, C 3-6 cycloalkyl, for example cyclopropyl, cyclobutyl or cyclopentyl preferably cyclopentyl, C 1-4 alkoxy for example methoxy or ethoxy, C 1-4 haloalkyl for example fluoromethyl, chloromethyl, trifluoromethyl, fluoroethyl, chloroethyl or trifluoroethyl, preferably trifluoroethyl or trifluoromethyl, and S(O) n R 10 for example methylsulphonyl or dimethyl amido sulphonyl.
• substituents selected from the group consisting of halo for example fluoro or chloro
• C 1-4 alkyl for
• R 7 , R 15 and R 16 groups which have then been so substituted include for example branched alkyl groups such as 2-methylbutyl, 3-methylbutyl, substituted sulphonyl groups such as methylsulphonylmethyl, methylsulphonylethyl, dimethylamidosulphonylmethyl and dimethylamidosulphonylethyl and substituted phenyl groups such as 4-chlorophenyl, 4-nitrophenyl, 4-fluorophenyl, 4-methoxyphenyl, 2,4-dichlorophenyl, 4-chlorophenylmethyl, 4-nitrophenylmethyl, 4-fluorophenylmethyl, 4-methoxyphenyl methyl, 2,4-dichlorophenylmethyl, 4-chlorophenylethyl, 4-nitro phenyl ethyl, 4-fluorophenylethyl, 4-methoxyphenylethyl, and 2,4-dichlorophenylethyl.
• R 15 and R 16 together with the nitrogen to which they are attached form a three to seven-membered saturated or unsaturated heterocyclic ring optionally containing one or more further N, O or S atoms it is preferred that the ring is a five or six membered ring, is saturated and comprises one further heteroatom selected from N, O or S.
• Suitable examples of such rings include pyrrolidinyl, pyrazolidinyl, imidazolinyl, thiazolidinyl, isoxazolidinyl, piperidinyl, piperazinyl, morpholinyl, or thiomorpholinyl.
• Preferred rings include pyrrolidinyl, thiazolidinyl, morpholinyl, or thiomorpholinyl. Such rings may optionally be further substituted with one or more groups, preferably selected from the group consisting of oxo, C(O)OH, halo for example fluoro or chloro, and C 1-4 alkyl for example methyl or ethyl preferably methyl.
• groups preferably selected from the group consisting of oxo, C(O)OH, halo for example fluoro or chloro, and C 1-4 alkyl for example methyl or ethyl preferably methyl.
• any heterocyclic sulphur atoms may be optionally substituted with one or more oxo groups to form for example 1,1-dioxothiazolidinyl or 1,1-dioxothiomorpholinyl substitutents.
• Suitable compounds include those where, when the R 6 group comprises a one carbon alkylene moiety, that said alkylene moiety is optionally substituted with one or two substituents. Further suitable compounds also include those where, when the R 6 group comprises a two carbon alkylene moiety, that said alkylene moiety is optionally substituted with one, two, three or four substituents which may be independently orientated on either the alpha or beta carbon positions with respect to the imidazole nitrogen to which the R 6 substitutent is bound.
• C 0-2 alkylene or C 1-2 alkylene of R 6 is substituted with one or more substitutents it is preferred that such substituents are independently selected from the group consisting of hydrogen; C 1-4 alkyl for example methyl or ethyl; C 3-6 cycloalkyl for example cyclopropyl; C 1-4 alkyleneC 3-6 cycloalkyl for example cyclopropylmethyl or cyclopropylethyl; C 1-4 alkoxy for example methoxy or ethoxy; C 1-4 alkyleneC 1-4 alkyoxy for example methoxy methyl, methoxy ethyl, ethoxy methyl or ethoxy ethyl; C 1-4 haloalkyl for example fluoromethyl, trifluromethyl, fluoroethyl or 1,1,1-trifluoroethyl; phenyl, benzyl and 4-trifluoromethylbenzyl.
• substituents are independently selected from the group
• substituents are independently chosen from the group consisting of hydrogen; C 1-4 alkyl for example methyl or ethyl; C 3-6 cycloalkyl for example cyclopropyl; C 1-4 alkyleneC 3-6 cycloalkyl for example cyclopropylmethyl or cyclopropylethyl; C 1-4 haloalkyl for example fluoromethyl, trifluromethyl, fluoroethyl or 1,1,1-trifluoroethyl; and phenyl.
• Suitable compounds include those where R 6 is selected from the group consisting of —C 0-2 alkyleneR 7 , preferably where R 6 is CH 2 R 7 , and where R 7 is selected from the group consisting of C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl; C 3-8 cycloalkyl for example cyclopropyl, cyclobutyl, cyclopentyl; C 1-6 haloalkyl for example trifluoromethyl, and trifluoroethyl; and C 0-6 alkylenephenyl for example phenyl which is optionally substituted to form for example 4-methoxy phenyl, 4-trifluoromethylphenyl.
• R 6 is selected from the group consisting of —C 0-2 alkyleneR 7 , preferably where R 6 does not comprise an additional alkylene moiety (ie is CoalkyleneR 7 ) 7
• R 7 is selected from the group consisting of C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, preferably methyl and ethyl; C 3-8 cycloalkyl for example cyclopropyl, cyclobutyl, cyclopentyl, preferably cyclopropyl; C 1-6 haloalkyl for example trifluoromethyl, and trifluoroethyl; and C 0-6 alkylenephenyl for example phenyl which is optionally substituted to form for example 4-methoxy phenyl, 4-trifluoromethylphenyl.
• a further group of suitable compounds include those where R 6 is selected from the group consisting of —C 1-2 alkyleneOR 7 , preferably where R 6 is CH 2 OR 7 , and where R 7 is selected from the group consisting of C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl.
• R 6 groups examples include methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, propoxymethyl, propoxyethyl, isopropoxyethyl, butoxymethyl, sec-butoxyoxymethyl, isobutoxymethyl, tert-butoxymethyl, butoxyethyl, sec-butoxyoxyethyl, isobutoxyethyl, tert-butoxyethyl, pentyloxymethyl, pentyloxyethyl, hexyloxymethyl, hexyloxyethyl.
• a still further group of suitable compounds include those where R 6 is selected from the group consisting of —C 1-2 alkyleneOC(O)R 7 , preferably where R 6 is CH 2 OC(O)R 7 , and where R 7 is C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, which R 7 in turn may be optionally further substituted.
• R 6 groups examples include acetyloxymethyl, acetyloxyethyl, propionyloxymethyl, propionyloxyethyl, butyryloxymethyl, butyryloxyethyl, isobutyryloxymethyl, isobutyryloxyethyl, pentanoyloxymethyl, pentanoyloxyethyl, 2-methylbutyryloxymethyl, 2-methylbutyryloxyethyl, 3-methylbutyryloxymethyl, 3-methylbutyrylcarbonyloxy)ethyl, 2,2-dimethylpropionyloxymethyl, 2,2-dimethylpropionyloxyethyl hexanoyloxymethyl, hexanoyloxyethyl, heptanoyloxymethyl, heptanoyloxyethyl.
• R 6 is selected from the group consisting of —C 1-2 alkyleneOC(O)R 7 , preferably where R 6 is CH 2 OC(O)R 7
• R 7 is C 1-4 alkylene(C 3-6 cycloalkyl) for example cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylpropyl, cyclohexylmethyl, and cyclcohexylethyl.
• R 6 groups examples include cyclopropylacetyloxymethyl, cyclopropylpropionyloxymethyl, cyclobutylacetyloxymethyl, cyclobutylpropionyloxymethyl, cyclopentylacetyloxymethyl, cyclopentylpropionyloxymethyl, cyclopentylbutyryloxymethyl, cyclohexylacetyloxymethyl, and cyclcohexylpropionyloxymethyl, cyclopropylacetyloxyethyl, cyclopropylpropionyloxyethyl, cyclobutylacetyloxyethyl, cyclobutylpropionyloxyethyl, cyclopentylacetyloxyethyl, cyclopentylpropionyloxyethyl, cyclopentylbutyryloxyethyl, cyclohexylacetyloxyethyl, and cyclcohexylpropion
• R 6 is 3-cyclopentylpropionyloxymethyl. It is preferred that in such compounds R 7 is preferably C 1-8 alkyl, more preferably ethyl or tert-butyl, and most preferably tert-butyl.
• a yet further group of suitable compounds include those where R 6 is selected from the group consisting of —C 1-2 alkyleneOC(O)OR 7 , preferably where R 6 is CH 2 OC(O)OR 7 , and where R 7 is C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, which may in turn be optionally further substituted.
• R 6 groups examples include methoxycarbonyloxymethyl, methoxycarbonyloxyethyl, ethoxycarbonyloxymethyl, ethoxycarbonyloxyethyl, propoxycarbonyloxymethyl, propoxycarbonyloxyethyl, isopropoxycarbonyloxymethyl, isopropoxycarbonyloxyethyl, butoxycarbonyloxymethyl, butoxycarbonyloxyethyl, isobutoxycarbonyloxymethyl, isobutoxycarbonyloxyethyl, pentyloxycarbonyloxymethyl, pentyloxycarbonyloxyethyl, 2-methylbutoxycarbonyloxymethyl, 2-methylbutoxycarbonyloxyethyl, 3-methylbutoxycarbonyloxymethyl, 3-methylbutoxycarbonyloxyethyl, 2,2-dimethylpropoxycarbonyloxymethyl, 2,2-dimethylpropoxycarbonyloxyethyl, hexyloxycarbonyloxymethyl, hexyloxycarbonyl
• R 6 is selected from the group consisting of —C 1-2 alkyleneOC(O)OR 7 , preferably where R 6 is CH 2 OC(O)OR 7
• R 7 is selected from the group consisting of C 3-6 cycloalkyl for example cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl
• C 1-4 alkylene(C 3-6 cycloalkyl) for example cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclohexylmethyl, cyclohexylethyl
• C 1-6 haloalkyl for example trifluoromethyl, and 2,2,2-trifluoroethyl
• C 0-6 alkylphenyl for example phenyl which is optionally further substituted to form for example 4-
• R 6 groups examples include cyclopropyloxycarbonyloxymethyl, cyclobutyloxycarbonyloxymethyl, cyclopentyloxycarbonyloxymethyl or cyclohexyloxycarbonyloxymethyl cyclopropyloxycarbonyloxyethyl, cyclobutyloxycarbonyloxyethyl, cyclopentyloxycarbonyloxyethyl or cyclohexyloxycarbonyloxyethyl; C 1-4 alkylene(C 3-6 cycloalkyl) for example cyclopropylmethyloxycarbonyloxymethyl, cyclopropylethyloxycarbonyloxymethyl, cyclobutylmethyloxycarbonyloxymethyl, cyclobutylethyloxycarbonyloxymethyl, cyclopentylmethyloxycarbonyloxymethyl, cyclopentylethyloxycarbonyloxymethyl, cyclohexylmethyloxycarbonyloxymethyl, cyclohehexyl
• a still yet further group of suitable compounds include those where R 6 is selected from the group consisting of —C 0-2 alkyleneC(O)OR 7 , preferably where R 6 is C(O)OR 7 , and where R 7 is C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, which may in turn be optionally further substituted.
• R 6 groups examples include methoxycarbonyl, methoxycarbonylmethyl, methoxycarbonylethyl, ethoxycarbonyl, ethoxycarbonylmethyl, ethoxycarbonylethyl, propoxycarbonyl, propoxycarbonylmethyl, propoxycarbonylethyl, isopropoxycarbonyl, isopropoxycarbonylmethyl, isopropoxycarbonylethyl, butoxycarbonyl, butoxycarbonylmethyl, butoxycarbonylethyl, isobutoxycarbonyl, isobutoxycarbonylmethyl, isobutoxycarbonylethyl, pentyloxycarbonyl, pentyloxycarbonylmethyl, pentyloxycarbonylethyl, 2-methylbutoxycarbonyl, 2-methylbutoxycarbonylmethyl, 2-methylbutoxycarbonylethyl, 3-methylbutoxycarbonyl, 3-methylbutoxycarbonylmethyl, 3-methylbutoxycarbonyl, 3-methylbutoxycarbonylmethyl, 3-methylbut
• R 6 is selected from the group consisting of —C 0-2 alkyleneC(O)OR 7 , preferably where R 6 is C(O)OR 7
• R 7 is selected from the group consisting of C 0-6 alkylphenyl for example phenyl which in turn is optionally substituted to form for example 4-methoxy phenyl, 4-trifluoromethyl phenyl.
• R 6 groups include phenyloxycarbonyl, phenyloxycarbonylmethyl, phenyloxycarbonylethyl.
• R 6 is selected from the group consisting of —C 1-2 alkyleneOC(O)NHR 7 , preferably where R 6 is CH 2 OC(O)NHR 7 , and where R 7 is selected from the group consisting of C 1-8 alkyl for example methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl; C 3-6 cycloalkyl for example cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; C 1-6 haloalkyl for example trifluoromethyl, and trifluoroethyl; and C 0-6 alkylphenyl for example phenyl, phenylmethyl or phenylethyl which C 0-6 alkylphenyl is optionally substituted to form for example 4-methoxyphenyl, 4-trifluoromethylphenyl, 2,4-dichlorophenyl
• R 6 is selected from the group consisting of hydrogen, —C 0-2 alkyleneR 7 and —C 1-2 alkyleneOC(O)R 7 and where R 7 is selected from the group consisting of C 1-8 alkyl. Even more preferred compounds are those where R 6 is hydrogen.
• each R 8 and R 9 are independently selected from the group consisting of hydrogen; C 1-4 alkyl eg methyl or ethyl, preferably methyl; C 1-4 haloalkyl for example trifluoromethyl, trichloromethyl, trichloroethyl or trifluoroethyl, preferably trifluoromethyl; C 1-4 alkoxy for example methoxy or ethoxy, preferably methoxy; and C 0-4 alkylenephenyl for example phenyl, phenylmethyl or phenylethyl, but with the proviso that R 8 and R 9 are not both hydrogen.
• each R 8 and R 9 are independently selected from the group consisting of hydrogen and C 1-4 alkyl eg methyl or ethyl, preferably methyl but again with the proviso that R 8 and R 9 are not both hydrogen. Most preferably R 8 is methyl and R 9 is hydrogen.
• R 8 or R 9 are phenyl
• the phenyl group is optionally substituted with one or more substitutents selected from the group consisting of fluoro, chloro, methoxy or trifluoromethyl.
• R 8 and R 9 together with the carbon to which they are attached may form a three to six membered carbocyclic, saturated ring it is preferred that the ring is a three membered ring.
• each of R 11 and R 12 are independently selected from the group consisting of hydrogen, C 1-2 alkyl eg methyl or ethyl, preferably methyl, and C 1-2 alkoxy for example methoxy or ethoxy, preferably methoxy. More preferably at least one of R 11 and R 12 is hydrogen. Most preferably both of R 11 and R 12 are hydrogen.
• a further group of suitable compounds of the present invention are those of formula (LV) where: each of R 1 , R 2 , R 3 , R 4 , R 5 are independently selected from hydrogen and C 1-4 alkyl eg methyl or ethyl, preferably methyl;
• a further group of preferred compounds are the compounds of formula (XXXX)
• R 1 to R 5 are selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl and CN, and R 8 is C 1-3 alkyl.
• at least two of R 1 to R 5 are hydrogen, and more preferably at least three of R 1 to R 5 are hydrogen.
• the groups from R 1 to R 5 that are not hydrogen are selected from chloro, fluoro, methyl, ethyl, difluoromethyl and trifluoromethyl, and more preferably from fluoro, chloro and methyl.
• R 8 is methyl or ethyl, and more preferably R 8 is methyl.
• a further group of preferred compounds are the compounds of formula (XXXXI)
• R 1 to R 5 are selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl and CN
• R 7 is phenyl optionally substituted by one or more groups selected from cyano, nitro, halo, formyl, hydroxy, C(O)OH, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, C 3-6 cycloalkyl, C 1-4 alkyleneC 3-6 cycloalkyl, C 1-4 alkoxy, —C(O)OC 1-4 alkyl, C 1-4 haloalkyl, C 1-4 haloalkoxy, pyrazolyl, triazolyl, amino, C 1-4 alkylamino, and C 1-4 dialkylamino
• R 8 is C 1-3 alkyl.
• R 1 to R 5 are hydrogen, and more preferably at least three of R 1 to R 5 are hydrogen.
• the groups from R 1 to R 5 that are not hydrogen are selected from chloro, fluoro, methyl, ethyl, difluoromethyl and trifluoromethyl, and more preferably from fluoro, chloro and methyl.
• R 7 is phenyl optionally substituted by one or two groups selected from cyano, chloro, fluoro, hydroxy, C 1-3 alkyl, C 1-3 alkoxy and C 1-2 haloalkyl.
• R 8 is methyl or ethyl, and more preferably R 8 is methyl.
• a further group of preferred compounds are the compounds of formula (XXXXII)
• R 1 to R 5 are selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl and CN
• R 7 is selected from C 1-3 alkylenephenyl optionally substituted by on the phenyl ring by one or more groups selected from cyano, halo, hydroxy, C(O)OH, C 1-4 alkyl, C 3-6 cycloalkyl, C 1-4 alkyleneC 3-6 cycloalkyl, C 1-4 alkoxy, —C(O)OC 1-4 alkyl, C 1-4 haloalkyl, and C 1-4 haloalkoxy, C 1-8 alkyl optionally substituted by one or two C 1-4 alkoxy groups, C 3-6 cycloalkyl, C 1-3 alkyleneC 3-6 cycloalkyl, and C 1-6 haloalkyl, and R 3 is C 1-3 alkyl.
• R 1 to R 5 are hydrogen, and more preferably at least three of R 1 to R 5 are hydrogen.
• the groups from R 1 to R 5 that are not hydrogen are selected from chloro, fluoro, methyl, ethyl, difluoromethyl and trifluoromethyl, and more preferably from fluoro, chloro and methyl.
• R 7 is C 1-8 alkyl or C 1-6 haloalkyl.
• R 8 is methyl or ethyl, and more preferably R 8 is methyl.
• a further group of preferred compounds are the compounds of formula (XXXXIII)
• R 1 to R 5 are selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl and CN
• R 7 is selected from C 1-3 alkylenephenyl optionally substituted by on the phenyl ring by one or more groups selected from cyano, halo, hydroxy, C(O)OH, C 1-4 alkyl, C 3-6 cycloalkyl, C 1-4 alkyleneC 3-6 cycloalkyl, C 1-4 alkoxy, —C(O)OC 1-4 alkyl, C 1-4 haloalkyl, and C 1-4 haloalkoxy, C 1-8 alkyl optionally substituted by one or two C 1-4 alkoxy groups, C 3-6 cycloalkyl, C 1-3 alkyleneC 3-6 cycloalkyl, and C 1-6 haloalkyl, and R 8 is C 1-3 alkyl.
• R 1 to R 5 are hydrogen, and more preferably at least three of R 1 to R 5 are hydrogen.
• the groups from R 1 to R 5 that are not hydrogen are selected from chloro, fluoro, methyl, ethyl, difluoromethyl and trifluoromethyl, and more preferably from fluoro, chloro and methyl.
• R 7 is C 1-8 alkyl or C 1-6 haloalkyl.
• R 8 is methyl or ethyl, and more preferably R 8 is methyl.
• a further group of preferred compounds are the compounds of formula (XXXXIV)
• R 1 to R 5 are selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl and CN
• R 7 is selected from C 1-3 alkylenephenyl optionally substituted by on the phenyl ring by one or more groups selected from cyano, halo, hydroxy, C(O)OH, C 1-4 alkyl, C 3-6 cycloalkyl, C 1-4 alkyleneC 3-6 cycloalkyl, C 1-4 alkoxy, —C(O)OC 1-4 alkyl, C 1-4 haloalkyl, and C 1-4 haloalkoxy, C 1-8 alkyl optionally substituted by one or two C 1-4 alkoxy groups, C 3-6 cycloalkyl, C 1-3 alkyleneC 3-6 cycloalkyl, and C 1-6 haloalkyl, and R 8 is C 1-3 alkyl.
• R 1 to R 5 are hydrogen, and more preferably at least three of R 1 to R 5 are hydrogen.
• the groups from R 1 to R 5 that are not hydrogen are selected from chloro, fluoro, methyl, ethyl, difluoromethyl and trifluoromethyl, and more preferably from fluoro, chloro and methyl.
• R 7 is C 1-8 alkyl or C 1-6 haloalkyl, and more preferably R 7 is isobutyl.
• R 8 is methyl or ethyl, and more preferably R 8 is methyl.
• Preferred individual compounds of the invention are selected from the compounds of the Examples described herein.
• More preferred individual compounds of the invention are selected from:
• More preferred individual compounds of the present invention are selected from:
• Even more preferred compounds of the present invention are 2-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, and ⁇ 2-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazol-1-yl ⁇ methyl pivalate, or a pharmaceutically acceptable salt or prodrug thereof.
• the most preferred compound of the present invention is 2-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, or a pharmaceutically acceptable salt or prodrug thereof.
• stereoisomers such as enantiomers and diasteromers, all geometric isomers and tautomeric forms of the compounds of formula (I), including compounds exhibiting more than one type of isomerism, and mixtures of one or more thereof.
• acid addition or base salts wherein the counterion is optically active for example, D-lactate or L-lysine, or racemic, for example, DL-tartrate or DL-arginine.
• compounds of formula (I) may contain one or more asymmetric carbon atoms, thus compounds of the invention can exist as two or more stereoisomers.
• R 8 and R 9 are different substitutents a stereocentre exists at the carbon atom to which they are attached—the benzylic carbon.
• Suitable compounds for use in this invention include those where the absolute stereochemistry at the benzylic carbon has the “S configuration”. Further suitable compounds for use in this invention include those where the absolute stereochemistry at the benzylic carbon has the “R configuration”. Such stereoisomers can be resolved and identified by one skilled in the art using known techniques.
• the present invention includes the individual stereoisomers of the compounds of formula (I) together with mixtures thereof.
• Preferred compounds of formula (I) include those of formula (IA) and formula (IB) which possess the stereochemistry shown below.
• preferred compounds are those of the formula (IA).
• preferred compounds are those of the formula (IB).
• Preferred compounds of the present invention include 2-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, 2-[(1R)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, ⁇ 2-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazol-1-yl ⁇ methylpivalate, ⁇ 2-[(1R)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazol-1-yl ⁇ methylpivalate or a pharmaceutically acceptable salt or prodrug thereof.
• Still more preferred compounds of the present invention are 2-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, 2-[(1R)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, or a pharmaceutically acceptable salt or prodrug thereof with the formulae shown below.
• Geometric isomers may be separated by conventional techniques well known to those skilled in the art, for example, chromatography and fractional crystallisation.
• racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where the compound of formula (I) contains an acidic or basic moiety, an acid or base such as tartaric acid or 1-phenylethylamine.
• a suitable optically active compound for example, an alcohol, or, in the case where the compound of formula (I) contains an acidic or basic moiety, an acid or base such as tartaric acid or 1-phenylethylamine.
• the resulting diastereomeric mixture may be separated by chromatography and/or fractional crystallization and one or both of the diastereoisomers converted to the corresponding pure enantiomer(s) by means well known to a skilled person.
• Chiral compounds of the invention may be obtained in enantiomerically-enriched form using chromatography, typically HPLC, on an asymmetric resin with a mobile phase consisting of a hydrocarbon, typically heptane or hexane, containing from 0 to 50% isopropanol, typically from 2 to 20%, and from 0 to 5% of an alkylamine, typically 0.1% diethylamine. Concentration of the eluant affords the enriched mixture.
• Stereoisomeric conglomerates may be separated by conventional techniques known to those skilled in the art—see, for example, “Stereochemistry of Organic Compounds” by E L Eliel (Wiley, New York, 1994).
• halo means a group selected from fluoro, chloro, bromo or iodo.
• Alkyl, alkylene, alkenyl, alkynyl and alkoxy groups, containing the requisite number of carbon atoms can be unbranched or branched.
• alkyl include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl and t-butyl.
• alkoxy include methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy and t-butoxy.
• alkylene include —CH 2 —, —CH(CH 3 )— and —C 2 H 4 —.
• cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.
• references to pharmaceutically acceptable compounds includes references to veterinarily acceptable compounds or agriculturally acceptable compounds.
• references to pharmaceutical activity includes references to veterinary activity or agricultural activity.
• Pharmaceutically acceptable salts of the compounds of formula (I) include the acid addition and base salts thereof. Suitable acid addition salts are formed from acids, which form non-toxic salts. Examples include the acetate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, borate, camsylate, citrate, edisylate, esylate, formate, fumarate, gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromide/bromide, hydroiodide/iodide, isethionate, lactate, malate, maleate, malonate, mesylate, methylsulphate, naphthylate, 2-napsylate, nicotinate, nitrate, orotate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/dihydrogen phosphate
• Suitable base salts are formed from bases which form non-toxic salts. Examples include the aluminium, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine and zinc salts.
• the pharmaceutically, veterinarily and agriculturally acceptable acid addition salts of certain of the compounds of formula (I) may also be prepared in a conventional manner.
• a solution of a free base may be treated with the appropriate acid, either neat or in a suitable solvent, and the resulting salt isolated either by filtration or by evaporation under reduced pressure of the reaction solvent.
• suitable salts see “Handbook of Pharmaceutical Salts: Properties, Selection, and Use” by Stahl and Wermuth (Wiley-VCH, Weinheim, Germany, 2002).
• the compounds of the invention may exist in both unsolvated and solvated forms.
• solvate is used herein to describe a molecular complex comprising the compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, ethanol.
• hydrate is employed when said solvent is water.
• Pharmaceutically acceptable solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e.g. D 2 O, d 6 -acetone, d 6 -DMSO.
• references to compounds of formula (I) include references to salts, solvates and complexes thereof and to solvates and complexes of salts thereof.
• the invention includes all polymorphs of the compounds of formula (I) as hereinbefore defined.
• complexes such as clathrates, drug-host inclusion complexes wherein, in contrast to the aforementioned solvates, the drug and host are present in stoichiometric or non-stoichiometric amounts.
• complexes of the drug containing two or more organic and/or inorganic components which may be in stoichiometric or non-stoichiometric amounts.
• the resulting complexes may be ionised, partially ionised, or non-ionised.
• the present invention includes all pharmaceutically acceptable isotopically-labelled compounds of formula (I) wherein one or more atoms are replaced by atoms having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
• isotopes suitable for inclusion in the compounds of the invention include isotopes of hydrogen, such as 2 H and 3 H, carbon, such as 11 C, 13 C and 14 C, chlorine, such as 36 Cl, fluorine, such as 18 F, iodine, such as 123 I and 125 I, nitrogen, such as 13 N and 15 N, oxygen, such as 15 O, 17 O and 18 O, phosphorus, such as 32 P, and sulphur, such as 35 S.
• prodrugs of the compounds of formula (I).
• certain derivatives of compounds of formula (I) which may have little or no pharmacological activity themselves can, when administered into or onto the body of an animal, be converted by the host or parasite into compounds of formula (I) having the desired activity, for example, by hydrolytic or enzymatic cleavage.
• prodrugs Such derivatives are referred to as ‘prodrugs’. It will be appreciated that certain compounds of formula (I) may themselves act as pro-drugs of other compounds of formula (I). Further information on the use of prodrugs may be found in ‘Pro-drugs as Novel Delivery Systems, Vol. 14, ACS Symposium Series (T Higuchi and W Stella) and ‘Bioreversible Carriers in Drug Design’, Pergamon Press, 1987 (ed. E B Roche, American Pharmaceutical Association).
• Prodrugs in accordance with the invention can, for example, be produced by replacing appropriate functionalities present in the compounds of formula (I) with certain moieties known to those skilled in the art as ‘pro-moieties’ as described, for example, in “Design of Prodrugs” by H Bundgaard (Elsevier, 1985).
• prodrugs in accordance with the invention include:
• Prodrugs in accordance with the invention can, for example, be produced by reacting compounds of formula (I) wherein R 6 is H with certain moieties known to those skilled in the art as ‘pro-drug moieties’ as described, for example, in “Design of Prodrugs” by H Bundgaard (Elsevier, 1985); “Design and application of prodrugs,” Textbook of Drug Design and Discovery, (3 Edition), 2002, 410-458, (Taylor and Francis Ltd., London); and references therein.
• substituents include: alkyl amines, aryl amines, amides, ureas, carbamates, carbonates, imines, enamines, imides, sulfenamides, and sulfonamides.
• the hydrocarbon portion of these groups contain C 1-6 alkyl, phenyl, heteroaryl such as pyridyl, C 2-6 alkenyl, and C 3-8 cycloalkyl; wherein each of the above groups may include one or more optional substituents where chemically possible independently selected from: halo; hydroxy; C 1-6 alkyl, C 1-6 haloalkyl and C 1-6 alkoxy.
• a prodrug that is administered to a test animal and metabolized by the host according to the invention can be readily identified by sampling a body fluid for a compound of formula (I).
• the present invention provides processes for the preparation of a compound of formula (I), or a pharmaceutically, veterinarily or agriculturally acceptable salt thereof, or a pharmaceutically, veterinarily or agriculturally acceptable solvate (including hydrate) of either entity, as illustrated below.
• R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 R 11 R 12 , R 15 and R 16 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 R 12 , R 15 and R 16 , are as defined for formula (I), are intended to optionally include suitably protected variants, P 1 , P 2 , P 3 , P 4 , P 5 , P 6 , P 7 , P 8 , P 9 , P 10 P 11 P 12 , P 15 and P 16 .
• protecting groups for these functionalities are described in the references listed below and the use of these protecting groups where needed is specifically intended to fall within the scope of the processes described in the present invention for producing compounds of formula (I) and its precursors. When suitable protecting groups are used, then these will need to be removed to yield compounds of formula (I). Deprotection can be effected according to standard procedures including those described in the references listed below.
• R 6 is a protecting group it is preferred that it is chosen from benzyl, p-methoxybenzyl, diethoxymethyl, allyl and trityl.
• Compounds of formula (I) may be obtained from other compounds of formula (I) by standard procedures such as electrophilic or nucleophilic substitution, organometallic catalysed cross coupling reactions and functional group interconversions known to those skilled in the art.
• compounds of formula (II) may be synthesised from compounds of formula (II) using standard hydrogenation procedures.
• compounds of formula (II) wherein R a is hydrogen, and R b is hydrogen or alkyl may be reduced to compounds of formula (I) in a suitable protic solvent such as methanol or propan-2-ol under a hydrogen atmosphere at temperatures up to 60° C. and elevated pressure up to 300 psi in the presence of 10% palladium on carbon or Freiborg activated 10% palladium on carbon for up to 72 h.
• a suitable protic solvent such as methanol or propan-2-ol
• compounds of formula (I) may be obtained from compounds of formula (II) by transfer hydrogenation conditions.
• ammonium formate or formic acid or ammonium formate in the presence of formic acid may be used to generate an in situ source of hydrogen which when in the presence of a hydrogenation catalyst such as 10% palladium on carbon in an alcoholic solvent such as propan-2-ol, for 2-3 hours at temperatures up to 80° C. can be used to effect the transformation of compounds of formula (II) to compounds of formula (I).
• a hydrogenation catalyst such as 10% palladium on carbon in an alcoholic solvent such as propan-2-ol
• reactions using formic acid as the hydrogen source may be performed without alcoholic solvents.
• Stereoselective hydrogenations may be performed to yield a preferred stereoisomer using chiral catalysts, in accordance with standard organic chemistry textbooks or literature precedent.
• chiral catalysts in accordance with standard organic chemistry textbooks or literature precedent.
• transition metals such as palladium, rhodium and ruthenium.
• One particularly preferred catalyst is bis(norbornadiene)rhodium(I) tetrafluoroborate.
• Enantiopure ligands that have been utilised to effect enantioselective hydrogenations have been referenced in the literature and illustrative examples of homochiral ligands include phospholanes such as Duphos and its analogues, ferrocenyl ligands such as Josiphos, 1-[(R)-2-diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine, biphenyl ligands such as (+/ ⁇ )-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene (BINAP) and miscellaneous ligands such as Prophos, Diamp, Bicp, Monophos.
• phospholanes such as Duphos and its analogues
• ferrocenyl ligands such as Josiphos, 1-[(R)-2-diphenylphosphino)ferrocenyl]
• references providing details of enantioselective hydrogenations include Y. Yamanori, T. Imamoto, Reviews on Heteroatom Chemistry, 1999, 20, 227; T. Clark, C. Landis, Tetrahedron: Asymmetry, 2004, 15, 14, 2123; H. Blaser, Topics in Catalysis, 2002, 19, 1, 3; H. Blaser et al, Synthetic Methods of organometallic and inorganic chemistry, 2002, 10, 78; Pure and Applied Chemistry, 1999, 71, 8, 1531; Pure and Applied Chemistry, 1998, 70, 8, 1477; U. Berens et al, Speciality Chemicals, 2000, 20, 6, 210; M. T. Reetz, Pure and Applied Chemistry, 1999, 71, 8, 1503; D.
• enantiomerically enriched compounds of formula (I) may be obtained from achiral compounds of formula (II) by stereoselective hydrogenation.
• compounds of formula (II) wherein R a is hydrogen, and R b is hydrogen or alkyl may be reduced to compounds of formula (I) in a suitable protic solvent such as methanol under a hydrogen atmosphere at ambient temperatures and elevated pressure up to 60 psi in the presence of a rhodium catalyst such as bis(norbornadiene)rhodium(I) tetrafluoroborate and chiral ligand such as 1-[(R)-2-diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine to give optically enriched compounds of formula (I).
• a suitable protic solvent such as methanol under a hydrogen atmosphere at ambient temperatures and elevated pressure up to 60 psi in the presence of a rhodium catalyst such as bis(norbornad
• Chiral resolution can be utilised to enhance the enantiomeric purity of compounds of formula (I).
• an acid salt can be enantioselectively formed upon addition of an enantiomerically pure chiral acid such as di-p-toluoyl-L-tartaric acid in a suitable protic solvent such as methanol.
• a suitable protic solvent such as methanol.
• one enantiomer preferentially forms a crystalline salt which can be removed by filtration whereas the other enantiomer remains in the mother liquor.
• a suitable base such as sodium hydroxide (1N)
• the enantiomers are resolved to give separated optically enriched compounds of formula (I).
• racemic compounds of formula (I) may be resolved using chiral HPLC procedures, known to those skilled in the art, to give enantiomerically pure compounds of formula (I).
• Imidazole ring formation can also be utilised to access compounds of formula (I), other synthetic methods are precedented in textbooks and the literature.
• One illustrative example is from desirably substituted phenylacetonitrile reactants, for example a compound such as 2-(2,3-dimethylphenyl)propanenitrile may be reacted with an appropriately substituted ethylenediamine for example, the p-toluenesulfonic acid salt of ethylenediamine at elevated temperatures ranging from 140°-180° C. to form the compound of formula (I) wherein R 1 , R 2 and R 8 are methyl and R 3 , R 4 , R 5 , R 6 and R 9 , R 11 and R 12 are hydrogen.
• imidazole ring formation is from the reaction of suitably 2-substituted 2-aryl-1,1-dibromoethenes and an appropriately substituted ethylenediamine at room temperature to give the intermediate 2-substituted 2-arylmethylimidazoline.
• Standard oxidation procedures such as Swern oxidation can transform the intermediate 2-substituted 2-arylmethylimidazoline into compounds of formula (I).
• Compounds of formula (II) may be prepared by Wittig chemistry by the reaction of a compound of formula (X) with the appropriate alkylphosphonium salt-derived phosphorus ylid.
• a compound of formula (X) for example treatment of a methyltriphenylphosphonium halide with a strong base in a suitable solvent, followed by the addition of (X), will produce a compound of formula (II) wherein both R a and R b are hydrogen.
• the base reagent is a solution of n-butyllithium in hexane, the solvent is ether or tetrahydrofuran and the reaction is conducted at from about room temperature to about 35° C.
• Compounds of formula (II) may undergo functional group interconversion into other compounds of formula (II). For example, wherein one or more of R 1 , R 2 , R 3 , R 4 and R 5 are bromo or iodo, and R 6 is protected with a suitable protecting group such as benzyl, palladium catalysed coupling reactions such as Stille, Heck and Suzuki coupling reactions may be effected.
• a suitable protecting group such as benzyl
• palladium catalysed coupling reactions such as Stille, Heck and Suzuki coupling reactions may be effected.
• organohalide compounds of formula (II) for example, treatment of such organohalide compounds of formula (II) with a suitable boronic acid such as an alkyl or aryl boronic acid, in an inert solvent such as toluene, in the presence of a suitable base such as potassium phosphate, a suitable phosphine ligand such as tricyclohexylphosphine and palladium acetate under an inert atmosphere at elevated temperatures up to 120° C. for up to 18 h provides the corresponding alkylated or arylated compound of formula (II).
• a suitable boronic acid such as an alkyl or aryl boronic acid
• an inert solvent such as toluene
• a suitable base such as potassium phosphate
• a suitable phosphine ligand such as tricyclohexylphosphine and palladium acetate
• compounds of formula (II) wherein one or more of R 1 , R 2 , R 3 , R 4 and R 5 are bromo or iodo, and R 6 is protected with a suitable protecting group such as benzyl may undergo transmetallation reaction with a palladium catalyst such as [1,1-bis(diphenylphosphino)ferrocene]palladium (II) chloride followed by cross coupling with a suitable boronic anhydride such as trialkylboroxine under an inert atmosphere, in the presence of a mild base such as sodium carbonate and a suitable inert solvent such as dioxane and water at elevated temperatures up to 120° C.
• a palladium catalyst such as [1,1-bis(diphenylphosphino)ferrocene]palladium (II) chloride
• a suitable boronic anhydride such as trialkylboroxine under an inert atmosphere
• a mild base such as sodium carbonate
• compounds of formula (II) wherein one or more of R 1 , R 2 , R 3 , R 4 and R 5 are bromo or iodo, and R 6 is protected with a suitable protecting group such as benzyl may undergo nucleophilic substitution reactions.
• nitrile compounds may be formed upon treatment of such a halo compound of formula (II) in a polar solvent such as N,N-dimethylacetamide with a cyanide source such as copper cyanide at temperatures up to 150° C.
• Nitrile compounds of formula (II) may also be formed from the corresponding halo compound of formula (II) upon treatment with a cyanide source such as sodium cyanide in the presence of a suitable transmetallating agent such as nickel bromide in a polar solvent such as N-methylpyrrolidinone and heating in a 150 W microwave at up to 150° C. for 5 min.
• a cyanide source such as sodium cyanide
• a suitable transmetallating agent such as nickel bromide in a polar solvent such as N-methylpyrrolidinone
• Nitrile compounds of formula (II) may also be formed from the corresponding halo compound of formula (II) from the reaction of a suitable cyanide source such as potassium hexacyanoferrate, a transmetallating agent such as copper iodide, a salt such as potassium iodide, and a coordinating agent such as dimethylethylenediamine in a polar solvent such as N-methylpyrrolidinone under an inert atmosphere at elevated temperatures up to 140° C. for up to 60 hours.
• a suitable cyanide source such as potassium hexacyanoferrate
• a transmetallating agent such as copper iodide
• a salt such as potassium iodide
• a coordinating agent such as dimethylethylenediamine
• R 6 may be a suitable protecting group e.g. benzyl, or substituted benzyl.
• dehydration may be effected under acidic conditions.
• compounds of formula (III) may be treated with an inorganic acid such as hydrochloric acid (4-6N) or concentrated sulphuric acid, for up to 72 h, optionally in an organic miscible solvent such as acetonitrile, optionally at elevated temperatures up to 60° C.
• dehydration may result from heating compounds of formula (III) at reflux with an organic acid such as trifluoroacetic acid or p-toluenesulphonic acid in an aprotic solvent such as toluene.
• compounds of formula (III) may be dehydrated using Eaton's reagent, typically stirring at room temperature for several hours neat or in a polar solvent such as methanol.
• Dehydration may also be effected by treating a compound of formula (III) with thionyl chloride in a polar solvent such as acetonitrile.
• Compounds of formula (III) may be used to directly access compounds of formula (I) upon treatment with Pearlman's catalyst in a suitable protic solvent such as methanol under a hydrogen atmosphere, in cases wherein R 6 is a benzylic protecting group a deprotected compound of formula (I) will be obtained wherein R 6 is hydrogen.
• compounds of formula (III) wherein R 6 is a protecting group such as benzyl may be deprotected, dehydrated and reduced simultaneously by hydrogenation under acidic conditions.
• Compounds of formula (II) may be obtained by dehydrohalogenation procedures, known to the skilled man, from compounds of formula (III) for example by standard chlorination followed by dehydrochlorination procedures.
• compounds of formula (II) can be obtained by transition metal catalysed cross-coupling reactions by utilizing methods known in the literature. For these reactions, it may be necessary to protect the basic imidazole, optionally R 6 may include a suitable protecting group such as diethoxymethyl.
• suitably protected organozincates such as compounds of formula (V), wherein X is halo for example chloro or bromo, can be coupled with suitably substituted styrenes such as compounds of formula (IV) wherein Y is a group suitable for transmetallation such as OTf, Cl, Br or I in the presence of a palladium catalyst such as Pd(PPh 3 ) 3 .
• Standard deprotection of compounds of formula (II) wherein R 6 is a suitable protecting group provides compounds of formula (II) in which R 6 is hydrogen.
• R 6 is diethoxymethyl treatment with an organic acid such as trifluoroacetic acid or an inorganic acid such as hydrochloric acid provides compound (II) wherein R 6 is hydrogen.
• deprotection of compounds of formula (II) wherein R 6 is a benzyl moiety protecting group may easily be effected by hydrogenation.
• Compounds of formula (III) wherein R 6 is a protecting group can be formed by 1,2-addition of a suitably protected organometallic compound (VI) to the corresponding ketone (VII) where chemically feasible for example wherein R 1 , R 2 , R 3 , R 4 and R 5 may be chosen independently from alkyl, chloro, and R a and R b may be chosen from alkyl.
• compound (VI) may be reacted with ketone (VII) in an aprotic solvent such as tetrahydrofuran at temperatures typically ranging from ⁇ 80 to 0° C. to give compounds of formula (III), which can be readily deprotected to give a compound of formula (III) wherein R 6 is H if desired.
• aprotic solvent such as tetrahydrofuran
• organometallic chemistry may be utilized to yield a compound of formula (III), wherein R 6 is a suitable protecting group such as benzyl, when an organometallic compound of formula (VIII), wherein X may be a halo e.g. chloro or bromo, is added to a ketone of formula (IX) wherein R 6 is a protecting group.
• R 6 is a suitable protecting group such as benzyl
• organometallic reagents include Grignard reagents and organolithium reagents.
• a Grignard reagent such as methylmagnesium chloride may be added to a solution of compound (X) in an anhydrous, aprotic solvent such as tetrahydrofuran, toluene or diethyl ether at ⁇ 10°-0° C. for up to 4 h to provide compounds of formula (III) wherein R a and R b are H.
• compounds of formula (IV), (V), (VI), (VII), (VIII), and (IX) may readily be accessed by utilisation of literature methods or simple modifications thereof as would be routinely employed by a skilled man.
• compounds of formula (V) can be prepared by stirring a 1-protected imidazole with n-butyllithium at reduced temperature, typically ⁇ 60 to ⁇ 20° C. followed by the addition of zinc chloride and allowing to warm to room temperature.
• compound (VI) may be obtained in situ by treatment of a protected imidazole reactant, with an organolithium reagent such as n-butylithium in an aprotic solvent such as tetrahydrofuran at reduced temperatures typically ranging from ⁇ 80 to 0° C.
• organolithium reagent such as n-butylithium
• aprotic solvent such as tetrahydrofuran
• compounds of formula (IX) may be synthesised by acylating a suitably substituted imidazole using acid chlorides.
• a suitable acid chloride with a 1-protected imidazole in the presence of a mild base such as triethylamine provides compounds of formula (IX).
• Compounds of formula (VII) may be prepared by the addition of a chelating agent such as Fe(acac) 3 and a Grignard reagent such as methylmagnesium bromide to a suitably substituted acid chloride (XI) at reduced temperatures, typically ⁇ 20° C. in a suitable aprotic solvent.
• Acid chlorides (XI) may be prepared by the reaction of the corresponding benzoic acid (XII) with thionyl chloride or oxalyl chloride, at elevated temperatures, typically 100° C. for several hours.
• Compounds of formula (VII) may also be prepared by reaction of an acid anhydride such as acetic anhydride, with a phenyl Grignard reactant (XIII) in an aprotic solvent.
• an acid anhydride such as acetic anhydride
• a phenyl Grignard reactant (XIII) in an aprotic solvent.
• amides, or acid chlorides may be used in place of the acid anhydride.
• Compounds of formula (XIII) may be formed in situ by reacting a suitable bromobenzene derivative with magnesium turnings in an anhydrous, aprotic solvent such as tetrahydrofuran.
• compounds of formula (VII) may be prepared by reacting a Grignard reactant e.g. methylmagnesium bromide with an amide e.g. a suitably substituted benzoylmorpholine (XIV) at reflux in a suitable solvent such as tetrahydrofuran.
• a Grignard reactant e.g. methylmagnesium bromide
• an amide e.g. a suitably substituted benzoylmorpholine (XIV)
• a suitable solvent such as tetrahydrofuran.
• Compounds of formula (VII) may also be obtained from reaction of a suitable benzoic acid (XII) with an organolithium reactant, for example methyllithium, at reduced temperatures in an anhydrous aprotic solvent such as tetrahydrofuran.
• a suitable benzoic acid (XII) with an organolithium reactant, for example methyllithium, at reduced temperatures in an anhydrous aprotic solvent such as tetrahydrofuran.
• Compounds of formula (VII) may be obtained by Friedel Crafts acylation of suitably functionalized phenyl moieties.
• a functionalized phenyl reactant can be treated with a Lewis acid such as aluminium chloride, in the presence of a suitable acylating agent such as acetyl chloride, in an aprotic solvent such as dichloromethane at room temperature for up to 18 h to give the desired compounds of formula (VII).
• compounds of formula (VII) may by obtained in a two step procedure from a suitably substituted halobenzene, preferably bromo or iodo benzene.
• a bromobenzene compound may be transmetallated with an organometallic reagent such as n-butyllithium in an anhydrous, apolar solvent such as tetrahydrofuran at low temperatures down to ⁇ 80° C.
• Compounds of formula (VII) may also be formed from the corresponding aryliodide and boronic acids using palladium chemistry in a carbon monoxide atmosphere.
• heating aryliodides with carbon monoxide, methylboronic acid and palladium tetrakis triphenylphosphine provides compounds of formula (VII) wherein R a and R b are H.
• Compounds of formula (VII) may undergo standard chemical reactions and functional group interconversion reactions known to the skilled man to give other compounds of formula (VII).
• compounds of formula (VII) may be chlorinated using standard reagents such as SelectafluorTM and sodium chloride.
• suitably substituted halo compounds of formula (VII) may undergo standard palladium catalysed cross coupling reactions such as Suzuki, Stille, Heck reactions to give a variety of standard products.
• bromo or iodo compounds of formula (VII) may undergo alkylation and arylation reactions via Suzuki coupling reactions upon treatment with an organoborane e.g.
• Compounds of formula (X) may be obtained from the reaction of acid chlorides of formula (XI) and imidazoles of formula (XV) wherein R 6 is a suitable protecting group in a suitable aprotic solvent such as toluene or acetonitrile in the presence of a mild base such as triethylamine at temperatures ranging from ⁇ 10°-130° C.
• Suitably functionalised acid chlorides of formula (XI) may be synthesized from the corresponding acid upon treatment with thionyl chloride at 80° C. for ⁇ 1 hour.
• acid chlorides may be synthesized from carboxylic acids upon treatment with oxalyl chloride in an aprotic solvent such as toluene at room temperature for up to 4 hours.
• Suitably functionalized acids may be obtained by utilising standard literature procedures available to the skilled man, thus substituents may be introduced via electrophilic or nucleophilic substitution or cross coupling reactions or via functional group interconversion.
• One such oxidation may include Dess Martin oxidation conditions.
• a compound of formula (X) may be prepared by stirring the corresponding compound of formula (XVI) at room temperature with Dess-Martin Periodinane in a suitable polar solvent such as dichloromethane.
• Compounds of formula (XVI) may be formed by the 1,2-addition of a suitably protected organometallic compound to a suitable aldehyde.
• a suitably protected organometallic compound to a suitable aldehyde.
• reaction of an organolithium compound of formula (VI) and a corresponding aldehyde of formula (XVII), in an anhydrous, aprotic solvent such as tetrahydrofuran at temperatures ranging from ⁇ 80-0° C. provides compounds of formula (XVI).
• L is a suitable leaving group such as Cl, Br, I, or a sulfonate such as trifluoromethanesulfonate.
• R 6 is hydrogen
• compounds of formula (I) wherein R 6 is hydrogen may be reacted with alkylating agents in the presence of a mild base such as cesium carbonate, potassium carbonate, triethylamine, or diisopropylethylamine, in an aprotic solvent such as acetone, 1-methyl-2-pyrrolidinone, dichloromethane, tetrahydrofuran, acetonitrile or N,N-dimethylformamide optionally in the presence of a salt such as sodium iodide.
• a mild base such as cesium carbonate, potassium carbonate, triethylamine, or diisopropylethylamine
• an aprotic solvent such as acetone, 1-methyl-2-pyrrolidinone, dichloromethane, tetrahydrofuran,
• Alkylating agents of the form Cl—CH 2 OC(O)R 7 may be produced from the reaction of the acid chloride ClC(O)R 7 with paraformaldehyde in the presence of a Lewis acid such as zinc chloride at temperatures up to 80° C. for 2-3 hours. Under alkylating conditions such reagents give compounds of formula (I) wherein R 6 is CH 2 OC(O)R 7 .
• Alkylating agents of the form L-CH 2 OC(O)OR 7 may be produced from the reaction of the alcohol HOR 7 with chloromethyl chloroformate in an aprotic solvent such as dichloromethane at temperatures ranging from 0° C. to room temperature. Under alkylating conditions such reagents give compounds of formula (I) wherein R 6 is CH 2 OC(O)OR 7 .
• Alkylating agents of the form L-CH 2 OC(O)NHR 7 may be produced from the reaction of the amine R 7 NH 2 with chloromethyl chloroformate in an aprotic solvent such as dichloromethane at temperatures ranging from ⁇ 10° C. to room temperature. Under alkylating conditions such reagents give compounds of formula (I) wherein R 6 is CH 2 OC(O)NHR 7 .
• Alkylating agents of the form L-CH 2 OC(O)NR 15 R 16 may be produced from the reaction of the amine R 15 R 16 NH with chloromethyl chloroformate in an aprotic solvent such as dichloromethane optionally in the presence of a mild base such as diisopropylethylamine at temperatures ranging from ⁇ 0° C. to room temperature. Under alkylating conditions such reagents give compounds of formula (I) wherein R 6 is CH 2 OC(O)NR 15 R 16 .
• Compounds of formula (I) wherein R 6 is hydrogen may be reacted with acylating agents of the formula ClC(O)R 7 , O[OC(O)R 7 ] 2 , ClC(O)OR 7 , ClC(O)NHR 7 , ClC(O)NR 15 R 16 , to provide compounds wherein R 6 is —C(O)R 7 , —OC(O)R 7 , —C(O)OR 7 , —C(O)NHR 7 , —C(O)NR 15 R 16 .
• compounds of formula (I) wherein R 6 is hydrogen may be reacted with acylating agents in the presence of a mild base such as triethylamine, or pyridine in an aprotic solvent such as dichloromethane, tetrahdyrofuran or acetonitrile at temperatures ranging from room temperature to 100° C. for between 1 and 36 h.
• a mild base such as triethylamine, or pyridine
• an aprotic solvent such as dichloromethane, tetrahdyrofuran or acetonitrile
• acylating agent ClC(O)OR 7 in situ.
• a compound of formula (I) wherein R 6 is hydrogen may be reacted with phosgene or diphosgene in an anhydrous solvent such as dichloromethane or acetonitrile in the presence of a mild base such as pyridine in the presence of an alcohol R 7 OH at ambient temperature to give the compound of formula (I) wherein R 6 is C(O)OR 7 .
• Compounds of formula (II) may be cyclopropanated to give compounds of formula (I) wherein R 8 and R 9 together form a cyclopropyl ring.
• Compounds of formula (II) may be reacted with a carbenoid species, CR d R e .
• a reactive species such as trimethylsilyl difluoro(fluorosulfonyl)acetate (TFDA) may be reacted with a compound of formula (II), with an optional apolar solvent at elevated temperature in the presence of sodium fluoride to yield a product of formula (I) after deprotection, wherein the cyclopropyl ring is substituted with fluoro.
• Other specific methods include treatment of chloroform with base, preferably under phase transfer catalysis conditions, thermolysis of a suitable organometallic precursor such as an aryl trifluoromethyl, trichloromethyl, or phenyl(trifluoromethyl) mercury derivative or treatment with a diazoalkane in the presence of a transition metal catalyst and treatment with a diazoalkane in the absence of a transition metal catalyst followed by thermolysis of the intermediate pyrazoline, or generation from a sulphur ylid.
• a suitable organometallic precursor such as an aryl trifluoromethyl, trichloromethyl, or phenyl(trifluoromethyl) mercury derivative
• treatment with a diazoalkane in the presence of a transition metal catalyst and treatment with a diazoalkane in the absence of a transition metal catalyst followed by thermolysis of the intermediate pyrazoline, or generation from a sulphur ylid.
• the present invention also relates to intermediates of formula (LX) below:
• the present invention also relates to intermediates of formula (LXV) below:
• the present invention also relates to intermediates of formula (LXX) below:
• Pg in the formulas (LX), (LXV) and (LXX) above can represent a wide range of possible protecting group and the specific group required will depend on the final compounds to be made and can be readily selected by one of ordinary skill.
• Preferred protecting groups include benzyl, para-methoxybenzyl, allyl, trityl, or 1,1-diethoxymethyl, preferably benzyl.
• This invention also relates to a pharmaceutical composition
• a pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, together with a pharmaceutically acceptable diluent or carrier, which may be adapted for oral, parenteral or topical administration.
• compositions suitable for the delivery of compounds of the present invention and methods for their preparation will be readily apparent to those skilled in the art. Such compositions and methods for their preparation may be found, for example, in ‘Remington's Pharmaceutical Sciences’, 19th Edition (Mack Publishing Company, 1995).
• Compounds of the invention intended for pharmaceutical use may be administered as crystalline or amorphous products. They may be obtained, for example, as solid plugs, powders, or films by methods such as precipitation, crystallization, freeze drying, or spray drying, or evaporative drying. Microwave or radio frequency drying may be used for this purpose.
• the methods by which the compounds may be administered include oral administration by capsule, bolus, tablet, powders, lozenges, chews, multi and nanoparticulates, gels, solid solution, films, sprays, or liquid formulation.
• Liquid forms include suspensions, solutions, syrups, drenches and elixirs.
• Such formulations may be employed as fillers in soft or hard capsules and typically comprise a carrier, for example, water, ethanol, polyethylene glycol, propylene glycol, methylcellulose, or a suitable oil, and one or more emulsifying agents and/or suspending agents.
• Liquid formulations may also be prepared by the reconstitution of a solid, for example, from a sachet. Oral drenches are commonly prepared by dissolving or suspending the active ingredient in a suitable medium.
• Compounds of the present invention may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs (or as any combination thereof).
• the compounds may be administered alone or in a formulation appropriate to the specific use envisaged, the particular species of host mammal being treated and the parasite involved. Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients.
• excipient is used herein to describe any ingredient other than the compound(s) of the invention. The choice of excipient will to a large extent depend on factors such as the particular mode of administration, the effect of the excipient on solubility and stability, and the nature of the dosage form.
• compositions useful for oral administration may be prepared by mixing the active ingredient with a suitable finely divided diluent and/or disintegrating agent and/or binder, and/or lubricant etc.
• suitable finely divided diluent and/or disintegrating agent and/or binder and/or lubricant etc.
• Other possible ingredients include anti-oxidants, colourants, flavouring agents, preservatives and taste-masking agents.
• the drug may make up from 1 wt % to 80 wt % of the dosage form, more typically from 5 wt % to 60 wt % of the dosage form.
• disintegrants include sodium starch glycolate, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, croscarmellose sodium, crospovidone, polyvinylpyrrolidone, methyl cellulose, microcrystalline cellulose, lower alkyl-substituted hydroxypropyl cellulose, starch, pregelatinised starch and sodium alginate.
• the disintegrant will comprise from 1 wt % to 25 wt %, preferably from 5 wt % to 20 wt % of the dosage form.
• Binders are generally used to impart cohesive qualities to a tablet formulation. Suitable binders include microcrystalline cellulose, gelatin, sugars, polyethylene glycol, natural and synthetic gums, polyvinylpyrrolidone, pregelatinised starch, hydroxypropyl cellulose and hydroxypropyl methylcellulose. Examples of diluents include lactose (monohydrate, spray-dried monohydrate, anhydrous and the like), mannitol, xylitol, dextrose, sucrose, sorbitol, microcrystalline cellulose, starch and dibasic calcium phosphate dihydrate.
• Oral formulations may also optionally comprise surface active agents, such as sodium lauryl sulfate and polysorbate 80, and glidants such as silicon dioxide and talc.
• surface active agents such as sodium lauryl sulfate and polysorbate 80
• glidants such as silicon dioxide and talc.
• surface active agents may comprise from 0.2 wt % to 5 wt % of the tablet, and glidants may comprise from 0.2 wt % to 1 wt % of the tablet.
• Lubricants include magnesium stearate, calcium stearate, zinc stearate, sodium stearyl fumarate, and mixtures of magnesium stearate with sodium lauryl sulphate.
• Lubricants generally comprise from 0.25 wt % to 10 wt %, preferably from 0.5 wt % to 3 wt % of the tablet.
• Exemplary tablets contain up to about 80% drug, from about 10 wt % to about 90 wt % binder, from about 0 wt % to about 85 wt % diluent, from about 2 wt % to about 10 wt % disintegrant, and from about 0.25 wt % to about 10 wt % lubricant.
• the compounds may be administered topically to the skin or mucosa, that is dermally or transdermally. This is a preferred method of administration and as such it is desirable to develop active compounds, which are particularly suited to such formulations.
• Typical formulations for this purpose include pour-on, spot-on, dip, spray, mousse, shampoo, powder formulation, gels, hydrogels, lotions, solutions, creams, ointments, dusting powders, dressings, foams, films, skin patches, wafers, implants, sponges, fibres, bandages and microemulsions. Liposomes may also be used.
• Typical carriers include alcohol, water, mineral oil, liquid petrolatum, white petrolatum, glycerin, polyethylene glycol and propylene glycol.
• Penetration enhancers may be incorporated—see, for example, J Pharm Sci, 88 (10), 955-958 by Finnin and Morgan (October 1999).
• Pour-on or spot-on formulations may be prepared by dissolving the active ingredient in an acceptable liquid carrier vehicle such as butyl digol, liquid paraffin or a non-volatile ester, optionally with the addition of a volatile component such as propan-2-ol.
• pour-on, spot-on or spray formulations can be prepared by encapsulation, to leave a residue of active agent on the surface of the animal, this effect may ensure that the compounds of formula (I) have increased persistence of action and are more durable, for example they may be more waterfast.
• Agents may be added to the formulations of the present invention to improve the persistence of such formulations on the surface of the animal to which they are applied, for example to improve their persistence on the coat of the animal. It is particularly preferred to include such agents in a formulation which is to be applied as a pour-on or spot-on formulation.
• agents acrylic copolymers and in particular fluorinated acrylic copolymers.
• a particular suitable reagent is ForaperleTM (Redline Products Inc, Texas, USA).
• Certain topical formulations may include unpalatable additives to minimize accidental oral exposure.
• Injectable formulations may be prepared in the form of a sterile solution, which may contain other substances, for example enough salts or glucose to make the solution isotonic with blood.
• Acceptable liquid carriers include vegetable oils such as sesame oil, glycerides such as triacetin, esters such as benzyl benzoate, isopropyl myristate and fatty acid derivatives of propylene glycol, as well as organic solvents such as pyrrolidin-2-one and glycerol formal.
• the formulations are prepared by dissolving or suspending the active ingredient in the liquid carrier such that the final formulation contains from 0.01 to 10% by weight of the active ingredient.
• the compounds can be administered parenterally, or by injection directly into the blood stream, muscle or into an internal organ.
• suitable means for parenteral administration include intravenous, intraarterial, intraperitoneal, intrathecal, intraventricular, intraurethral, intrasternal, intracranial, intramuscular and subcutaneous.
• Suitable devices for parenteral administration include needle (including microneedle) injectors, needle-free injectors and infusion techniques.
• Parenteral formulations are typically aqueous solutions which may contain excipients such as salts, carbohydrates and buffering agents (preferably to a pH of from 3 to 9), but, for some applications, they may be more suitably formulated as a sterile non-aqueous solution or as powdered a dried form to be used in conjunction with a suitable vehicle such as sterile, pyrogen-free water.
• a suitable vehicle such as sterile, pyrogen-free water.
• the preparation of parenteral formulations under sterile conditions for example, by lyophilisation, may readily be accomplished using standard pharmaceutical techniques well known to those skilled in the art.
• the solubility of compounds of formula (I) used in the preparation of parenteral solutions may be increased by the use of appropriate formulation techniques, such as the incorporation of solubility-enhancing agents.
• Such formulations are prepared in a conventional manner in accordance with standard medicinal or veterinary practice.
• compositions will vary with regard to the weight of active compound contained therein, depending on the species of host animal to be treated, the severity and type of infection and the body weight of the host.
• typical dose ranges of the active ingredient are 0.01 to 100 mg per kg of body weight of the animal.
• Preferably the range is 0.1 to 10 mg per kg.
• Formulations may be immediate and/or modified controlled release.
• Controlled release formulations include modified release formulations including delayed-, sustained-, pulsed-, controlled, targeted, or programmed release. Suitable modified release formulations for the purposes of the invention are described in U.S. Pat. No. 6,106,864. Details of other suitable release technologies such as high energy dispersions and osmotic and coated particles are to be found in Verma et al, Pharmaceutical Technology On-line, 25(2), 1-14 (2001). The use of chewing gum to achieve controlled release is described in WO 00/35298.
• compounds of the invention may be formulated as a solid, semi-solid, or thixotropic liquid for administration as an implanted depot providing modified release of the active compound. Examples of such formulations include drug-coated stents and PGLA microspheres.
• the compounds may be administered to a non-human animal with the feedstuff and for this purpose a concentrated feed additive or premix may be prepared for mixing with the normal animal feed.
• All the aforementioned aqueous dispersions or emulsions or spraying mixtures can be applied, for example, to crops by any suitable means, chiefly by spraying, at rates which are generally of the order of about 100 to about 1,200 liters of spraying mixture per hectare, but may be higher or lower (eg. low or ultra-low volume) depending upon the need or application technique.
• the compounds or compositions according to the invention are conveniently applied to vegetation and in particular to roots or leaves having pests to be eliminated.
• Another method of application of the compounds or compositions according to the invention is by chemigation, that is to say, the addition of a formulation containing the active ingredient to irrigation water.
• This irrigation may be sprinkler irrigation for foliar pesticides or it can be ground irrigation or underground irrigation for soil or for systemic pesticides.
• the concentrated suspensions which can for example be applied by spraying, are prepared so as to produce a stable fluid product which does not settle (fine grinding) and usually contain from about 10 to about 75% by weight of active ingredient, from about 0.5 to about 30% of surface-active agents, from about 0.1 to about 10% of thixotropic agents, from about 0 to about 30% of suitable additives, such as anti-foaming agents, corrosion inhibitors, stabilizers, penetrating agents, adhesives and, as the carrier, water or an organic liquid in which the active ingredient is poorly soluble or insoluble. Some organic solids or inorganic salts may be dissolved in the carrier to help prevent settling or as antifreezes for water.
• the wettable powers are usually prepared so that they contain from about 10 to about 80% by weight of active ingredient, from about 20 to about 90% of a solid carrier, from about 0 to about 5% of a wetting agent, from about 3 to about 10% of a dispersing agent and, when necessary, from about 0 to about 80% of one or more stabilizers and/or other additives, such as penetrating agents, adhesives, anti-caking agents, colorants, or the like.
• the active ingredient(s) is(are) thoroughly mixed in a suitable blender with additional substances which may be impregnated on the porous filler and is(are) ground using a mill or other suitable grinder. This produces wettable powders, the wettability and the suspendability of which are advantageous. They may be suspended in water to give any desired concentration and this suspension can be employed very advantageously in particular for application to plant foliage.
• the “water dispersible granules (WG)” (granules which are readily dispersible in water) have compositions which are substantially close to that of the wettable powders. They may be prepared by granulation of formulations described for the wettable powders, either by a wet route (contacting finely divided active ingredient with the inert filler and a little water, e.g. 1 to 20% by weight, or with an aqueous solution of a dispersing agent or binder, followed by drying and screening), or by a dry route (compacting followed by grinding and screening).
• WG water dispersible granules
• compositions for application to control arthropod, plant nematode, helminth or protozoan pests usually contain from about 0.00001% to about 95%, more particularly from about 0.0005% to about 50% by weight of one or more compounds of formula (I), or pesticidally acceptable salts thereof, or of total active ingredients (that is to say the compound of formula (I), or a pesticidally acceptable salt thereof, together with: other substances toxic to arthropods or plant nematodes, anthelmintics, anticoccidials, synergists, trace elements or stabilizers).
• the actual compositions employed and their rate of application will be selected to achieve the desired effect(s) by the farmer, livestock producer, medical or veterinary practitioner, pest control operator or other person skilled in the art.
• the compounds of the invention may be combined with soluble macromolecular entities, such as cyclodextrin and suitable derivatives thereof or polyethylene glycol-containing polymers, in order to improve their solubility, dissolution rate, taste-masking, bioavailability and/or stability for use in any of the aforementioned modes of administration.
• soluble macromolecular entities such as cyclodextrin and suitable derivatives thereof or polyethylene glycol-containing polymers
• Drug-cyclodextrin complexes are found to be generally useful for most dosage forms and administration routes. Both inclusion and non-inclusion complexes may be used.
• the cyclodextrin may be used as an auxiliary additive, i.e. as a carrier, diluent, or solubiliser. Most commonly used for these purposes are alpha-, beta- and gamma-cyclodextrins, examples of which may be found in International Patent Applications Nos. WO 91/11172, WO 94/02518 and WO 98/55148.
• Compounds of the invention can also be mixed with one or more biologically active compounds or agents including insecticides, acaricides, anthelmintics, fungicides, nematocides, antiprotozoals, bactericides, growth regulators, entomopathogenic bacteria, viruses or fungi to form a multi-component pesticide giving an even broader spectrum of pharmaceutical, veterinary or agricultural utility.
• the present invention also pertains to a composition comprising a biologically effective amount of compounds of the invention and an effective amount of at least one additional biologically active compound or agent and can further comprise one or more of surfactant, a solid diluent or a liquid diluent.
• Specific further active compounds include those described in International Patent Application No WO0 2005/090313, at pages 39 to 44.
• compositions may conveniently be combined in the form of a kit suitable for coadministration of the compositions.
• the kit of the invention comprises two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (I) in accordance with the invention, and means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet.
• a container, divided bottle, or divided foil packet An example of such a kit is the familiar blister pack used for the packaging of tablets, capsules and the like.
• the kit of the invention is particularly suitable for administering different dosage forms, for example, oral and parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another.
• the kit typically comprises directions for administration and may be provided with a so-called memory aid.
• the compounds of the invention i.e. those of formula (I), possess parasiticidal activity in humans, animals, insects and plants. They are particularly useful in the treatment of ectoparasites.
• This invention also relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, or a pharmaceutical composition containing any of the foregoing, for use as a medicament.
• a further aspect of this invention relates to the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, for the manufacture of a medicament for the treatment of a parasitic infestation.
• this invention is useful for the manufacture of a medicament for the treatment of a parasitic infestation in humans.
• this invention is useful for the manufacture of a medicament for the treatment of a parasitic infestation in animals.
• this invention is useful for the manufacture of a medicament for the treatment of a parasitic infestation in insects.
• this invention is useful for the manufacture of a medicament for the treatment of a parasitic infestation in plants.
• An even further aspect of this invention relates to a method of treating a parasitic infestation in a mammal which comprises treating said mammal with an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, or a pharmaceutical composition containing any of the foregoing.
• a yet further aspect of this invention relates to a method of preventing a parasitic infestation in a mammal which comprises treating said mammal with an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, or a pharmaceutical composition containing any of the foregoing.
• this invention also relates to a method of controlling disease transmission in a mammal which comprises treating said mammal with an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate of either entity, or a pharmaceutical composition containing any of the foregoing.
• a method for the control of arthropod, plant nematode or helminth pests at a locus which comprises the treatment of the locus (e.g. by application or administration) with an effective amount of a compound of general formula (I), or a pesticidally acceptable salt thereof.
• references herein to “treatment” as used herein includes references to curative, palliative and prophylactic treatment, references to “control” (of parasites and/or pests etc.) include kill, repel, expel, incapacitate, deter, eliminate, alleviate, minimise, eradicate.
• the compounds of the invention have utility in the control of arthropod pests. They may, in particular, be used in the fields of veterinary medicine, livestock husbandry and the maintenance of public health: against arthropods which are parasitic internally or externally upon vertebrates, particularly warm-blooded vertebrates, including man and domestic animals such as dogs, cats, cattle, sheep, goats, equines, swine, poultry and fish for example Acarina , including ticks (e.g. Ixodes spp., Boophilus spp. e.g. Boophilus microplus, Amblyomma spp., Hyalomma spp., Rhipicephalus spp. e.g.
• arthropods which are parasitic internally or externally upon vertebrates, particularly warm-blooded vertebrates, including man and domestic animals such as dogs, cats, cattle, sheep, goats, equines, swine, poultry and fish for example Acarina , including ticks (e.
• Rhipicephalus appendiculatus Haemaphysalis spp., Dermacentor spp., Omithodorus spp. (e.g. Omithodorus moubata ), mites (e.g. Damalinia spp., Dermanyssus gallinae, Sarcoptes spp. e.g. Sarcoptes scabiei, Psoroptes spp., Chorioptes spp., Demodex spp., Eutrombicula spp.), specific further arthropod pests include those described in International Patent Application No WO 2005/090313 ; Diptera (e.g.
• the compounds of the present invention also have utility in the field of control of plant pests, soil inhabiting pests and other environmental pests.
• the present invention is particularly useful in the control of arthropod pests in mammals, in particular humans and animals.
• this invention is useful in the control of arthropod pests in animals which includes livestock such as cattle, sheep, goats, equines, swine and companion animals such as dogs and cats.
• the compounds of the invention are of particular value in the control of arthropods which are injurious to, or spread or act as vectors of diseases in, man and domestic animals, for example those hereinbefore mentioned, and more especially in the control of ticks, mites, lice, fleas, midges and biting, nuisance and myiasis flies. They are particularly useful in controlling arthropods which are present inside domestic host animals or which feed in or on the skin or suck the blood of the animal, for which purpose they may be administered orally, parenterally, percutaneously or topically.
• the compounds of the invention are of value for the treatment and control of the various lifecycle stages of parasites including egg, nymph, larvae, juvenile and adult stages.
• a method for the control of arthropod pests of insects which comprises treatment of the insect with an effective amount of a compound of general formula (I), or a pesticidally acceptable salt thereof.
• Compounds of the present invention may also be used for the treatment of infections caused by mites, and in particular varoaa mites.
• compounds of the present invention may also be used for the treatment of varoaa mite infection in bees.
• a method for the control of arthropod pests of plants which comprises treatment of the plant with an effective amount of a compound of general formula (I), or a pesticidally acceptable salt thereof.
• the compounds of the invention also have utility in the control of arthropod pests of plants.
• the active compound is generally applied to the locus at which the arthropod infestation is to be controlled at a rate of about 0.005 kg to about 25 kg of active compound per hectare (ha) of locus treated, preferably 0.02 to 2 kg/ha. Under ideal conditions, depending on the pest to be controlled, the lower rate may offer adequate protection. On the other hand, adverse weather conditions and other factors may require that the active ingredient be used in higher proportions. For foliar application, a rate of 0.01 to 1 kg/ha may be used.
• the locus is the plant surface, or the soil around the plant to be treated.
• a method for the protection of timber which comprises treatment of the timber with an effective amount of a compound of general formula (I), or a pesticidally acceptable salt thereof.
• Compounds of the present invention are also valuable in the protection of timber (standing, felled, converted, stored or structural) from attack by sawflies or beetles or termites. They have applications in the protection of stored products such as grains, fruits, nuts, spices and tobacco, whether whole, milled or compounded into products, from moth, beetle and mite attack. Also protected are stored animal products such as skins, hair, wool and feathers in natural or converted form (e.g.
• Solid or liquid compositions for application topically to timber, stored products or household goods usually contain from about 0.00005% to about 90%, more particularly from about 0.001% to about 10%, by weight of one or more compounds of formula (I) or pesticidally acceptable salts thereof.
• liquid compositions of this invention may, in addition to normal agricultural use applications be used for example to treat substrates or sites infested or liable to infestation by arthropods (or other pests controlled by compounds of this invention) including premises, outdoor or indoor storage or processing areas, containers or equipment or standing or running water.
• the present invention also relates to a method of cleaning animals in good health comprising the application to the animal of compound of formula (I) or a veterinarily acceptable salt.
• the purpose of such cleaning is to reduce or eliminate the infestation of humans with parasites carried by the animal and to improve the environment in which humans inhabit.
• the biological activity of the compounds was tested using one or more of the test methods outlined below.
• octopamine agonists to acarids for example, ticks, causes distinct behavioural changes compared to untreated control ticks. Treated ticks become agitated and move constantly, this prevents ticks attaching and feeding on a host animal to which the compound has been applied. Normal behaviour of ticks is to go into stasis when all other external stimuli are removed. Agitation and movement can be measured in vitro in the laboratory to predict efficacy and potency in vivo.
• the assay was run using unfed Rhipicephalus sanguineus (brown dog tick) and precoated glass vials with an inner surface area of 34.5 cm 2 . Each compound was tested in duplicate.
• agonist activity of compounds against insect octopamine receptors expressed in CHO cells could be determined by adapting the methods described in B. Maqueira, H. Chatwin, P. D. Evans, J. Neurochemistry, 2005, 94, 2, 547.
• the wedge and dashed bonds indicate absolute stereochemistry as drawn at this chiral centre
• a wiggly bond indicates that the absolute stereochemistry is unknown but the compound is a single stereoisomer at this chiral centre.
• Straight bonds emanating from a chiral centre indicate that the stereoisomers are not resolved and a mixture of stereoisomers is present.
• Optical rotation data was collected using a Perkin Elmer Polarimeter 341 by Warwick analytical Service, (University of Warwick Science Park, Barclays Venture Centre, Sir William Lyons Road, Coventry, CV4 7EZ).
• Example 2 The compound of Example 1 (750 mg, 3.75 mmol) was dissolved in ethanol (4 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 50 ⁇ 50 mm ID Chiralcel OD, 20 ⁇ m column, 50 ml/min) using ethanol:hexane [10:90] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (370 mg).
• the combined acidic aqueous layer was adjusted to pH 10 by addition of aqueous sodium hydroxide solution (1N) and the resulting precipitate was collected by filtration and dried in vacuo, at 50° C., to give the title compound (optical purity 98.58%).
• the process of di-p-toluoyl-L-tartaric acid salt formation and generation of free base was repeated once more to give the title compound (0.359 kg, optical purity 99.66%) after second resolution.
• Example 2 The compound of Example 1 (750 mg, 3.75 mmol) was dissolved in ethanol (4 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 50 ⁇ 50 mm ID Chiralcel OD, 20 ⁇ m column, 50 ml/min) using ethanol:hexane [10:90] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (370 mg).
• Example 20 The compound of Example 20 (40 mg, 0.22 mmol) was dissolved in ethanol (1 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 250 ⁇ 20 mm ID Chiralpak AD-H, 5 ⁇ m column, 15 ml/min) using ethanol:hexane [5:95] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (16 mg).
• Example 20 The compound of Example 20 (40 mg, 0.22 mmol) was dissolved in ethanol (1 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 250 ⁇ 20 mm ID Chiralpak AD-H, 5 ⁇ m column, 15 ml/min) using ethanol:hexane [5:95] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (15 mg).
• Example 76 The compound of Example 76 (540 mg, 1.8 mmol) was dissolved in ethanol (2 ml) and hexane (2 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 50 ⁇ 50 mm ID Chiralcel OD, 20 ⁇ m column, 40 ml/min) using ethanol:hexane [5:95] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (240 mg).
• Example 76 The compound of Example 76 (540 mg, 1.8 mmol) was dissolved in ethanol (2 ml) and hexane (2 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 50 ⁇ 50 mm ID Chiralcel OD, 20 ⁇ m column, 40 ml/min) using ethanol:hexane [5:95] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (260 mg).
• Example 7 The compound of Example 7 (18 mg, 0.09 mmol) was dissolved in ethanol:hexane (1:1, 2 ml) and the enantiomers were separated by automated preparative liquid chromatography (Gilson system, 250 ⁇ 20 mm ID Chiralcel OD-H, 5 ⁇ m column, 15 ml/min) using ethanol:hexane [5:95] as the mobile phase. The appropriate fractions were combined and concentrated to give the title compound (7 mg).
• the filtrate was purified by automated preparative liquid chromatography (Gilson system, 150 mm ⁇ 22.4 mm LUNA C18(2) 5 ⁇ m column, 20 ml/min) using an acetonitrile:water gradient [50:50 (15 min) to 98:2 (20 min)]. The appropriate fractions were combined and concentrated to give the title compound (31 mg).
• Example 58 To a mixture of the preparation of Example 58 (50 mg, 0.25 mmol) and caesium carbonate (203 mg, 0.62 mmol) in acetonitrile (2.5 ml) was added 1,1,1-trifluoro-3-iodopropane (73 ⁇ l, 0.62 mmol). The reaction mixture was heated at 100° C. in a microwave (200 W) for 45 min and then concentrated in vacuo. To the residue was added water (10 ml) and the mixture was extracted with ethyl acetate (2 ⁇ 10 ml). The combined extracts were dried (MgSO 4 ) and concentrated in vacuo.
• Example 58 To a mixture of Example 58 (500 mg, 2.5 mmol) and pyridine (0.44 ml, 5.5 mmol) in anhydrous dichloromethane (5 ml), at 0° C. and under nitrogen, was added phosgene (20% in toluene, 1.44 ml, 2.75 mmol). The mixture was stirred at 0° C. for 20 min, before addition of 1,3-diethoxypropan-2-ol (407 mg, 2.75 mmol). The reaction mixture was stirred at room temperature for 30 min and then poured into ice water (10 ml). The mixture was adjusted to pH 7 by addition of solid sodium hydrogen carbonate and the two layers were separated. The aqueous phase was extracted with dichloromethane (2 ⁇ 10 ml) and the combined extracts were dried (MgSO 4 ) and concentrated in vacuo.
• Example 58 To a mixture of the compound of Example 58 (100 mg, 0.5 mmol) and pyridine (90 ⁇ l, 1.1 mmol) in anhydrous acetonitrile (1 ml), at 0° C. and under nitrogen, was added diphosgene (33 ⁇ l, 0.28 mmol). The mixture was stirred at 0° C. for 30 min, before addition of cyclopropylmethanol (43 ⁇ l, 0.55 mmol). The reaction mixture was stirred at room temperature for 1 h and then filtered.
• the filtrate was purified by automated preparative liquid chromatography (Gilson system, 150 mm ⁇ 22.4 mm LUNA C18(2) 5 ⁇ m column, 20 ml/min) using an acetonitrile:water gradient [15:85 (3 min) to 98:2 (16 min)]. The appropriate fractions were combined and concentrated to give the title compound (30 mg).

Landscapes

• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Veterinary Medicine (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Animal Behavior & Ethology (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Tropical Medicine & Parasitology (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Chemical & Material Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

Priority Applications (4)

Applications Claiming Priority (2)

Related Child Applications (3)

Publications (2)

Family

ID=38038547

Family Applications (4)

Family Applications After (3)

Country Status (32)

Cited By (3)

Families Citing this family (17)

Citations (18)

Family Cites Families (5)

• 2007
  • 2007-01-04 US US11/619,735 patent/US7592362B2/en active Active
  • 2007-01-08 CN CN2007800026033A patent/CN101370786B/zh not_active Expired - Fee Related
  • 2007-01-08 AT AT07700025T patent/ATE505461T1/de active
  • 2007-01-08 ME MEP-42/08A patent/MEP4208A/xx unknown
  • 2007-01-08 AU AU2007206698A patent/AU2007206698B2/en not_active Ceased
  • 2007-01-08 BR BRPI0707185A patent/BRPI0707185B8/pt not_active IP Right Cessation
  • 2007-01-08 CA CA2632771A patent/CA2632771C/en not_active Expired - Fee Related
  • 2007-01-08 EP EP07700025A patent/EP1981853B1/en active Active
  • 2007-01-08 PL PL07700025T patent/PL1981853T3/pl unknown
  • 2007-01-08 MY MYPI20082647A patent/MY145812A/en unknown
  • 2007-01-08 PT PT07700025T patent/PT1981853E/pt unknown
  • 2007-01-08 UA UAA200809432A patent/UA93696C2/ru unknown
  • 2007-01-08 JP JP2008550864A patent/JP4463317B2/ja not_active Expired - Fee Related
  • 2007-01-08 DK DK07700025.5T patent/DK1981853T3/da active
  • 2007-01-08 WO PCT/IB2007/000071 patent/WO2007083207A1/en active Application Filing
  • 2007-01-08 ES ES07700025T patent/ES2362935T3/es active Active
  • 2007-01-08 EA EA200870079A patent/EA015738B1/ru not_active IP Right Cessation
  • 2007-01-08 RS RS20080304A patent/RS53512B1/en unknown
  • 2007-01-08 EP EP11161432A patent/EP2423199A1/en not_active Withdrawn
  • 2007-01-08 NZ NZ569209A patent/NZ569209A/en not_active IP Right Cessation
  • 2007-01-08 ME MEP-2008-42A patent/ME00044B/me unknown
  • 2007-01-08 DE DE602007013869T patent/DE602007013869D1/de active Active
  • 2007-01-08 KR KR1020087017642A patent/KR101044494B1/ko active IP Right Grant
  • 2007-01-08 SI SI200730644T patent/SI1981853T1/sl unknown
  • 2007-01-17 UY UY30096A patent/UY30096A1/es not_active Application Discontinuation
  • 2007-01-17 AR ARP070100202A patent/AR059055A1/es not_active Application Discontinuation
  • 2007-01-18 TW TW096101915A patent/TWI337998B/zh not_active IP Right Cessation
  • 2007-11-26 US US11/945,064 patent/US7547718B2/en active Active
  • 2007-11-26 US US11/945,083 patent/US7544706B2/en active Active
• 2008
  • 2008-06-11 IL IL192063A patent/IL192063A0/en not_active IP Right Cessation
  • 2008-06-25 ZA ZA200805565A patent/ZA200805565B/xx unknown
  • 2008-07-18 TN TNP2008000306A patent/TNSN08306A1/fr unknown
  • 2008-07-18 MA MA31128A patent/MA30166B1/fr unknown
  • 2008-08-04 NO NO20083404A patent/NO341141B1/no not_active IP Right Cessation
• 2009
  • 2009-06-19 HK HK09105506.7A patent/HK1127919A1/xx not_active IP Right Cessation
  • 2009-08-04 US US12/535,373 patent/US7825149B2/en not_active Expired - Fee Related
• 2011
  • 2011-05-17 CY CY20111100485T patent/CY1111473T1/el unknown

Patent Citations (18)

Non-Patent Citations (10)

Also Published As